Copegus and haemoglobin decreased Patient Reports February 12, 2012

Copegus Side Effects Report #5308020-X
Copegus side effect was reported by a Physician from UNITED STATES on Dec 12, 2005. Male patient, 54 years of age, was diagnosed with hepatitis c , anaemia of chronic disease and was treated with Copegus. After drug was administered, patient experienced the following side effects: haemoglobin decreased. Copegus dosage: unknown. During the same period patient was treated with PEGASYS, PROCRIT. Patient recovered.

Copegus Side Effects Report #4896605-4
Copegus side effect was reported by a Physician from UNITED STATES on Nov 21, 2005. Male patient, 54 years of age, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: haemoglobin decreased. Copegus dosage: unknown. During the same period patient was treated with PEGASYS. Patient recovered.

Copegus Side Effects Report #4713430-5
Copegus side effect was reported by a Health Professional from UNITED STATES on July 13, 2004. Female patient, 53 years of age, weighting 177.0 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, alpha 1 foetoprotein increased, aspartate aminotransferase increased, globulins increased, haematocrit decreased, haemoglobin decreased, lymphocyte count decreased, mean cell haemoglobin concentration decreased, neutrophil count decreased. Copegus dosage: unknown. During the same period patient was treated with PEGASYS. Patient recovered.

Copegus Side Effects Report #5284873-9
Copegus side effect was reported by a Health Professional from CANADA on Mar 27, 2007. Female patient, 51 years of age, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: enterocolitis haemorrhagic, haemoglobin decreased. Copegus dosage: unknown. During the same period patient was treated with PEGASYS. Patient was hospitalized. Patient recovered.


Copegus Side Effects Report #6082319-4
Copegus side effect was reported by a Health Professional from UNITED STATES on Jan 03, 2008. Male patient, 47 years of age, weighting 246.0 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood bilirubin increased, fatigue, haematocrit decreased, haemoglobin decreased, neutrophil count decreased, no therapeutic response. Copegus dosage: 1400 MG DAILY ORAL. During the same period patient was treated with INFERGEN, NADOLOL, FUROSEMIDE, OMEPRAZOLE, LISINOPRIL. Patient recovered.

Copegus Side Effects Report #5157779-3
Copegus side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2005. Female patient, 46 years of age, weighting 300.0 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: anaemia, blood glucose decreased, dyspnoea, fatigue, haemoglobin decreased, loss of consciousness, refusal of treatment by patient, syncope. Copegus dosage: unknown. During the same period patient was treated with TYLENOL. Patient was hospitalized and became disabled. Patient recovered.